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Completed

NCT Number: NCT03111017

Mechanisms and Management of Exercise Intolerance in Older Heart Failure Patients

Heart failure with preserved ejection fraction (HFpEF) is the fastest growing form of heart failure with a high morbidity and mortality rate, and is associated with severe exercise intolerance. The mechanisms responsible for the reduced exercise tolerance remain poorly understood. The investigators propose a novel paradigm shift, focusing on peripheral limitations to exercise. In particular, the investigators will test the hypothesis that muscle sympathetic nerve activity (MSNA) is elevated in older HFpEF patients compared to healthy controls, and is associated with reduced exercise tolerance. The investigators will also test whether 16-weeks of exercise training will lower MSNA compared to attention control, and correlate with improved exercise tolerance in older HFpEF patients.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Texas at Arlington

Arlington, Texas, 76019, United States

About this study

Heart failure with preserved ejection fraction is the fastest growing form of heart failure, is almost exclusively found in older persons, particularly older women, and is associated with a high morbidity and mortality rate. The primary chronic symptom in HFpEF patients is severe exercise intolerance measured objectively as decreased peak exercise oxygen uptake (peak VO2). A consequence of the reduced exercise tolerance is that activities of daily living require near maximal effort, resulting in further deconditioning and reduced quality of life. The majority of work to date has focused on cardiac limitations, showing impaired cardiac output and marked diastolic dysfunction. Although these findings have provided important insight into the pathophysiology of HFpEF, drug therapies targeting cardiac function do not improve peak VO2, quality of life, or survival in HFpEF patients.

Older HFpEF patients have multiple skeletal muscle abnormalities including reduced skeletal muscle oxidative capacity and capillary-to-fiber ratio resulting in increased anaerobic metabolism during low-level exercise. Importantly, accumulation of anaerobic metabolites within the exercising muscles are known to activate skeletal muscle afferent fibers (called metaboreceptors), that elicit a reflex-mediated increase in efferent muscle sympathetic (vasoconstrictor) nerve activity (MSNA). The investigators here propose a novel paradigm of exercise intolerance in older HFpEF patients whereby skeletal muscle abnormalities lead to overactivation of the muscle metaboreflex and MSNA mediated vasoconstriction that limits delivery of oxygenated blood to the active muscles. Further, exercise training mediated improvements in skeletal muscle function will alleviate the metaboreflex, thereby reducing MSNA and improve oxygen delivery to the contracting muscles.

To test this novel paradigm, the investigators will first perform an initial cross-sectional comparison of older (≥60 years) HFpEF patients (N=24) with age and sex-matched healthy controls (N=24), and then enter the HFpEF patients into a randomized, controlled, single blind, trial of exercise training to test the following hypothesis: (i) that MSNA is elevated in older HFpEF patients compared to healthy controls, and is associated with reduced peak VO2, physical functional performance, aerobic endurance, muscle blood flow, and quality of life; and (ii) Exercise training will attenuate MSNA compared to attention control, and will correlate with improved peak VO2, physical functional performance, aerobic endurance, muscle blood flow, and quality of life in older HFpEF patients.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for Heart Failure Preserved Ejection Fraction Patients:

  • ≥60 years of age, male or female.
  • Documented heart failure diagnosis.
  • Left ventricular ejection fraction ≥50%.
  • Clinically stable (no heart failure hospitalization within prior month).

Inclusion criteria

for Healthy Controls:

  • ≥60 years of age, male or female (matched to the age and sex of HFpEF patients).
  • No cardiac medications except for statins.
  • Sedentary (exercise three days per week or less).

Exclusion criteria

for Heart Failure Preserved Ejection Fraction Patients:

  • Greater than moderate valvular disease or congenital heart disease.
  • New York Heart Association class IV.
  • Any orthopedic or medical condition that would limit exercise testing or training.
  • Development of signs and symptoms of myocardial ischemia (1 mm ST segment depression on EKG), or unstable hemodynamics/rhythm, or systolic/diastolic blood pressure >240/110 mmHg during baseline cardiopulmonary (peak VO2) testing.

Exclusion criteria

for Healthy Controls:

  • Chronic medical condition (e.g. self reported hypertension, or diabetes, or chronic obstructive pulmonary disease or heart disease)
  • Abnormal history or cardiovascular physical exam.
  • Segmental wall motion abnormalities or structural valvular abnormalities.
  • Left ventricular ejection fraction <50%.
  • Any orthopedic or medical condition that would limit exercise testing.
  • Development of signs and symptoms of myocardial ischemia (1 mm ST segment depression on EKG), or unstable hemodynamics/rhythm, or systolic/diastolic blood pressure >240/110 mmHg during baseline cardiopulmonary (peak VO2) testing.

Treatment and study plan

Exercise training

Other

HFpEF patients randomized to either 16 weeks of exercise training or attention control group.

Primary outcomes

  1. Muscle sympathetic nerve activity (MSNA) assessed by direct microneurography

    Time frame: Change from Baseline MSNA at 16 weeks

    Standard microneurographic procedures will be used to directly measure MSNA, at rest and during handgrip exercise and post-exercise cuff occlusion, using the peroneal nerve.

Secondary outcomes

  1. Peak Oxygen Uptake (Peak VO2) assessed by gas exchange indirect calorimetry

    Time frame: Change from Baseline Peak VO2 at 16 weeks.

    Peak VO2 will be measured as the highest oxygen uptake during a peak cycle exercise test on an upright cycle ergometer.

  2. Physical functional performance assessed by Short Physical Performance Battery (SPPB) Test

    Time frame: Change from Baseline physical functional performance at 16 weeks.

    The Short Physical Performance Battery consists of 3 subtasks: standing balance, walking speed, and time to raise from a chair 5 times.

  3. Aerobic endurance assessed by six-minute walk distance

    Time frame: Change from Baseline aerobic endurance at 16 weeks.

    The six-minute walk test is a validated measure of aerobic endurance in patients with heart failure that measures the distance covered in a 6 min period.

  4. Muscle blood flow assessed by brachial artery Doppler Ultrasound

    Time frame: Change from Baseline muscle blood flow at 16 weeks.

    Measurement of brachial artery diameter and blood velocity via Doppler Ultrasound to calculate blood flow.

  5. Quality of life assessed by Kansas City Cardiomyopathy Questionnaire (KCCQ)

    Time frame: Change from Baseline quality of life at 16 weeks.

    The KCCQ is a valid, reliable and responsive health status measure for patients with heart failure.

Sponsors and collaborators

Lead sponsor

The University of Texas at Arlington

Other

Registry information

Official study title

Mechanisms and Management of Exercise Intolerance in Older Heart Failure Patients With Preserved Ejection Fraction

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Apr 12, 2017
Registry last updated
Mar 3, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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